Home LiteratureArticle Details
PMID: 19086053 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Identification of new putative susceptibility genes for several psychiatric disorders by association analysis of regulatory and non-synonymous SNPs of 306 genes involved in neurotransmission and neurodevelopment.

Gratacòs M, Costas J, de Cid R, Bayés M, González JR, Baca-García E, de Diego Y, Fernández-Aranda F, Fernández-Piqueras J, Guitart M, Martín-Santos R, Martorell L, Menchón JM, Roca M, Sáiz-Ruiz J, Sanjuán J, Torrens M, Urretavizcaya M, Valero J, Vilella E, Estivill X, Carracedo A, Psychiatric Genetics Network Group

Abstract

A fundamental difficulty in human genetics research is the identification of the spectrum of genetic variants that contribute to the susceptibility to common/complex disorders. We tested here the hypothesis that functional genetic variants may confer susceptibility to several related common disorders. We analyzed five main psychiatric diagnostic categories (substance-abuse, anxiety, eating, psychotic, and mood disorders) and two different control groups, representing a total of 3,214 samples, for 748 promoter and non-synonymous single nucleotide polymorphisms (SNPs) at 306 genes involved in neurotransmission and/or neurodevelopment. We identified strong associations to individual disorders, such as growth hormone releasing hormone (GHRH) with anxiety disorders, prolactin regulatory element (PREB) with eating disorders, ionotropic kainate glutamate receptor 5 (GRIK5) with bipolar disorder and several SNPs associated to several disorders, that may represent individual and related disease susceptibility factors. Remarkably, a functional SNP, rs945032, located in the promoter region of the bradykinin receptor B2 gene (BDKRB2) was associated to three disorders (panic disorder, substance abuse, and bipolar disorder), and two additional BDKRB2 SNPs to obsessive-compulsive disorder and major depression, providing evidence for common variants of susceptibility to several related psychiatric disorders. The association of BDKRB2 (odd ratios between 1.65 and 3.06) to several psychiatric disorders supports the view that a common genetic variant could confer susceptibility to clinically related phenotypes, and defines a new functional hint in the pathophysiology of psychiatric diseases.

MeSH Terms
Case-Control Studies Genes Genetic Linkage Genetic Predisposition to Disease/genetics Humans Mental Disorders/genetics,physiopathology Molecular Epidemiology Neurogenesis/genetics Polymorphism, Single Nucleotide/genetics Receptor, Bradykinin B2/genetics Synaptic Transmission/genetics
Chemicals
Receptor, Bradykinin B2
Authors & Affiliations
23 authors, click to expand affiliations / ORCID
Gratacòs Mònica
CIBER en Epidemiología y Salud Pública (CIBERESP), Instituto de Salud Carlos III, Madrid, Spain.
Costas Javier
de Cid Rafael
Bayés Mònica
González Juan R
Baca-García Enrique
de Diego Yolanda
Fernández-Aranda Fernando
Fernández-Piqueras José
Guitart Miriam
Martín-Santos Rocío
Martorell Lourdes
Menchón José M
Roca Miquel
Sáiz-Ruiz Jerónimo
Sanjuán Julio
Torrens Marta
Urretavizcaya Mikel
Valero Joaquín
Vilella Elisabet
Estivill Xavier
Carracedo Angel
Psychiatric Genetics Network Group
Article Info
Journal
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
Abbr.
Am J Med Genet B Neuropsychiatr Genet
ISSN
1552-485X
Published
2009-09-05
Pages
808-16
Language
English
Region
United States
NLM ID
101235742
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]